Canonical Allele Identifier: CA519357762

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154182240T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154953965T>G , CM000685.2:g.154953965T>G	GRCh38
NC_000023.10:g.154182240T>G , CM000685.1:g.154182240T>G	GRCh37
NC_000023.9:g.153835434T>G	NCBI36
NG_011403.1:g.73759A>C
NG_011403.2:g.73759A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1830A>C MANE Select	ENSP00000353393.4:p.Ile610=
ENST00000647125.1:c.*1706A>C	ENSP00000496062.1:n.*1706A>C
ENST00000360256.8:c.1830A>C	ENSP00000353393.4:p.Ile610=
NM_000132.3:c.1830A>C	NP_000123.1:p.Ile610=
XM_011531126.1:c.1725A>C	XP_011529428.1:p.Ile575=
NM_000132.4:c.1830A>C MANE Select	NP_000123.1:p.Ile610=